Towards Novel Treatments for Schizophrenia: Molecular and Behavioural Signatures of the Psychotropic Agent SEP-363856.
Veronica BegniAlice SansonAlessia LuoniFederica SensiniBen GraysonSyeda MunniJoanna C NeillMarco Andrea RivaPublished in: International journal of molecular sciences (2021)
Schizophrenia is a complex psychopathology whose treatment is still challenging. Given the limitations of existing antipsychotics, there is urgent need for novel drugs with fewer side effects. SEP-363856 (SEP-856) is a novel psychotropic agent currently under phase III clinical investigation for schizophrenia treatment. In this study, we investigated the ability of an acute oral SEP-856 administration to modulate the functional activity of specific brain regions at basal levels and under glutamatergic or dopaminergic-perturbed conditions in adult rats. We found that immediate-early genes (IEGs) expression was strongly upregulated in the prefrontal cortex and, to a less extent, in the ventral hippocampus, suggesting an activation of these regions. Furthermore, SEP-856 was effective in preventing the hyperactivity induced by an acute injection of phencyclidine (PCP), but not of d-amphetamine (AMPH). The compound effectively normalized the PCP-induced increase in IEGs expression in the PFC at all doses tested, whereas only the highest dose determined the major modulations on AMPH-induced changes. Lastly, SEP-856 acute administration corrected the cognitive deficits produced by subchronic PCP administration. Taken together, our data provide further insights on SEP-856, suggesting that modulation of the PFC may represent an important mechanism for the functional and behavioural activity of this novel compound.
Keyphrases
- prefrontal cortex
- drug induced
- liver failure
- bipolar disorder
- respiratory failure
- phase iii
- poor prognosis
- clinical trial
- aortic dissection
- high glucose
- open label
- diabetic rats
- randomized controlled trial
- spinal cord
- binding protein
- hepatitis b virus
- oxidative stress
- machine learning
- spinal cord injury
- cerebral ischemia
- mass spectrometry
- extracorporeal membrane oxygenation
- high resolution
- deep brain stimulation
- acute respiratory distress syndrome
- phase ii
- study protocol
- artificial intelligence
- functional connectivity
- genome wide identification